Mannosidase Deficiency Diseases
Diseases caused by the loss of one or more enzymes involved in the hydrolysis of mannoside linkages (MANNOSIDASES). The defects in enzyme activity are primarily associated with genetic mutation of the genes that codes for a particular mannosidase isoenzyme.
Year introduced: 2004
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Subheadings:
Tree Number(s): C16.320.565.202.607, C16.320.565.595.577, C18.452.648.202.607, C18.452.648.595.577
MeSH Unique ID: D044904
Entry Terms:
- Deficiency Disease, Mannosidase
- Deficiency Diseases, Mannosidase
- Diseases, Mannosidase Deficiency
- Mannosidase Deficiency Disease
- Mannosidase Deficiency Syndromes
- Deficiency Syndrome, Mannosidase
- Deficiency Syndromes, Mannosidase
- Mannosidase Deficiency Syndrome
- Mannosidosis
- Mannosidoses
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